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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866918Generated: October 30, 2026

Ammonia → 9-Cyano 10,11-dihydro-11-oxo-dibenzo[b,f]thiepin

https://huagongshe.com/reaction/866918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant1-chlorodibenzo[b,f]thiepin-10(11H)-oneHCID 827045—
ReactantHCID 178418260HCID 178418260—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
Product9-Cyano 10,11-dihydro-11-oxo-dibenzo[b,f]thiepinHCID 1268708527.9%

Reaction Conditions

Temperature200 °C

Reaction Steps

The mixture of 2.6g of 9-chloro-10,11-dihydro-11-oxo-dibenzo-[b,f]thiepin, 2.0g of copper cyanide, 0.1g of anhydrous copper sulfate and 50ml of N-methyl pyrrolidone was heated with stirring at 200° C overnight in a flask equipped with a tube packed with silica gel. After cooling, to the reaction mixture were added 100ml of conc. aqueous ammonia and 200ml of water, and the resulting mixture was extracted with benzene. The extract was washed with water, diluted hydrochloric acid and then water, which was dried over potassium sulfate and the solvent evaporated therefrom. The residue thus obtained was chromatographed on 200g of silica gel, and eluted with chloroform/methanol (50/1). 0.6g of the starting material was recovered from a first eluate. Recrystallization of the residue of a second eluate from benzene gave 0.7g of 9-cyano 10,11-dihydro-11-oxo-dibenzo[b,f]thiepin as pale yellow prismatic crystals having a melting point of 165°-167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101667
Source datasetuspto-grants-1978_07
ORD IDord-3d05fa2ffaee460caf237e748256a230
Source noteuspto-grants-1978_07